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R.G. Sutherland

Researcher at University of Saskatchewan

Publications -  43
Citations -  605

R.G. Sutherland is an academic researcher from University of Saskatchewan. The author has contributed to research in topics: Cyclopentadienyl complex & Hexafluorophosphate. The author has an hindex of 15, co-authored 43 publications receiving 586 citations.

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The effect of ultrasound on water in the presence of dissolved gases

TL;DR: In this paper, a sonolysis of water at 447 kHz causes a decrease in the pH and the products formed depend to some extent on the nature of the dissolved gases; products observed are hydrogen peroxide, nitrous and nitri...
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Some ring replacement and nucleophilic substitution reactions of η6-subsituted arene-η5-cylopentadienyliron hexafluorophosphates

TL;DR: A number of nitroarene and aminoarene complexes, including the PF 6 − salts of NO 2 C 6 H 5 FeCp p+, when heated with an excess of P(OC 2 H 5 ) 3 all gave rise to the ring replacement product, CpFe(P(O 2 H 4 ) 3 ) 3+PF 6 − (I).
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Ligand exchange of some heterocyclic analogues of fluorene and anthracene with ferrocene

TL;DR: In this article, the preparation of new complexes of the type (heteroarene)(cyclopentadienyl)iron hexafluorophosphate and (heterorene)bis(cyclopentadiyliron)-bis(hexafluorsophosphates) are described where heterorene is dibenzofuran or carbazole.
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Ligand exchange reactions between ferrocene and 9,10-dimethylanthracene

TL;DR: The reaction of 9,10-dimethylanthracene (8) with ferrocene (FcH) in the presence of AlCl3-Al in decalin gave the stereospecific hydrogenated product, η6-cis-(endo-9, 10-dihydro)-9,10 -dimethylthracenes-η5-cyclopentadienyliron cation (10a), the hydrogenation at C-9-10 being cis and endo or on the same side as the cyclopentad
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Studies on nucleophilic substitution reactions with η6-o-dichlorobenzene-η5-cyclopentadienyliron hexafluorophosphate

TL;DR: In this article, it was shown that IPF 6 with an excess of phenol or p-thiocresol in the presence of K 2 CO 3 could give disubstitution of both chloro groups of I, while a similar reaction with one equivalent of the nucleophile, and under conditions of high dilution, monosubstititution of only one of the chloro group of I could be obtained, while di- or monosUBstitution could be brought about under appropriate conditions with benzyl or methyl alcohol as the source of the nucleus